Pyridine → HCID 58529921, compound

HRID 2141576Notes

Reaction equation

HRID 2141576 reaction equation
[NH2:1][c:2]1[n:3][cH:4][n:5][n:6]2[c:7]1[c:8](-[c:19]1[cH:20][cH:21][c:22]3[cH:23][n:24]([CH2:28][c:29]4[cH:30][cH:31][cH:32][cH:33][cH:34]4)[n:25][c:26]3[cH:27]1)[cH:9][c:10]2-[c:11]1[cH:12][c:13]([CH2:17][OH:18])[cH:14][cH:15][cH:16]1.[O:45]1[CH2:46][CH2:47][O:48][CH2:49][CH2:50]1.[S:35]([Cl:36])([Cl:37])=[O:38].[cH:39]1[cH:40][cH:41][n:42][cH:43][cH:44]1>>[NH2:1][c:2]1[n:3][cH:4][n:5][n:6]2[c:7]1[c:8](-[c:19]1[cH:20][cH:21][c:22]3[cH:23][n:24]([CH2:28][c:29]4[cH:30][cH:31][cH:32][cH:33][cH:34]4)[n:25][c:26]3[cH:27]1)[cH:9][c:10]2-[c:11]1[cH:12][c:13]([CH2:17][Cl:37])[cH:14][cH:15][cH:16]1

Participants

5

Reactant 4

HCID 1049PyridineHCID 24386Thionyl ChlorideHCID 312751,4-DioxaneHCID 58529400HCID 58529400, compound

Product 1

HCID 58529921HCID 58529921, compound

Sources & evidence

ORD record
ord-0a3b86508e22490195a20ae3232c1240
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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